Evidence map›Paper›PMID 30650011›Full record

ArticleMolecular biology of the cell2019

A computational model of the early stages of acentriolar meiotic spindle assembly.

Gaelle Letort, Isma Bennabi, Serge Dmitrieff, François Nedelec, Marie-Hélène Verlhac, Marie-Emilie Terret

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Molecular design principles for bipolar spindle organization by two opposing motors.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Self-Organization of Cellular Units.Annual review of cell and developmental biology · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Gaelle LetortCIRB, Collège de France, UMR7241/U1050, F-75005 Paris, France.
Isma BennabiCIRB, Collège de France, UMR7241/U1050, F-75005 Paris, France.
Serge DmitrieffInstitut Jacques Monod, UMR7592 and Université Paris-Diderot, F-75205 Paris, France.
François NedelecCentre de Recherche Interdisciplinaire, F-75004 Paris, France.
Marie-Hélène VerlhacCIRB, Collège de France, UMR7241/U1050, F-75005 Paris, France.
Marie-Emilie TerretCIRB, Collège de France, UMR7241/U1050, F-75005 Paris, France.
Collège de France · FRCenter for Research and Interdisciplinarity · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mitotic spindle is an ensemble of microtubules responsible for the repartition of the chromosomal content between the two daughter cells during division. In metazoans, spindle assembly is a gradual process involving dynamic microtubules and recruitment of numerous associated proteins and motors. During mitosis, centrosomes organize and nucleate the majority of spindle microtubules. In contrast, oocytes lack canonical centrosomes but are still able to form bipolar spindles, starting from an initial ball that self-organizes in several hours. Interfering with early steps of meiotic spindle assembly can lead to erroneous chromosome segregation. Although not fully elucidated, this process is known to rely on antagonistic activities of plus end- and minus end-directed motors. We developed a model of early meiotic spindle assembly in mouse oocytes, including key factors such as microtubule dynamics and chromosome movement. We explored how the balance between plus end- and minus end-directed motors, as well as the influence of microtubule nucleation, impacts spindle morphology. In a refined model, we added spatial regulation of microtubule stability and minus-end clustering. We could reproduce the features of early stages of spindle assembly from 12 different experimental perturbations and predict eight additional perturbations. With its ability to characterize and predict chromosome individualization, this model can help deepen our understanding of spindle assembly.

Indexed as

AnimalsCell Nucleus DivisionCentrosomeChromosomesChromosome SegregationComputational BiologyComputer SimulationFemaleMiceMicrotubule-Associated ProteinsMicrotubulesMitosisModels, BiologicalOocytesSpindle ApparatusMicrotubule-Associated Proteins

Identifiers

PMID30650011
PMCPMC6589792
OpenAlexW2910305526

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.